2.1
The probability interpretation of the wavefunction
The wavefunction is not the shape of the particle, nor a density of particle stuff. It is a complex function, and only its modulus squared connects to experiment.
Recommended first
After this section you should be able to
- State the relation between Ψ, |Ψ|² and what an experiment actually measures
- Use the Born rule to compute the probability of finding a particle in a given interval
- Say precisely what is wrong with "an electron is a diffuse cloud"
The last chapter ended in an awkward place: de Broglie says particles have a wavelength, and the double slit says electrons really do interfere. So — what is waving?
In a water wave it is the height of the surface; in sound it is air pressure; in an electromagnetic wave it is the electric and magnetic fields. All of those can be measured directly. What about an electron wave? When Schrödinger wrote his equation in 1926 he had no answer either. He guessed that the wavefunction described the actual smeared-out distribution of the electron’s charge in space. That guess was disproved almost immediately.
The right answer came from Max Born, the same year, in a footnote.
The Born rule
Precisely: for a particle in the state , one position measurement returns a result in with probability
Here , because is generally complex. We call
the probability density. Watch its dimensions: in one dimension it is , so itself is not a probability — is.
The picture
Imagine you could repeat the same experiment a hundred million times: prepare an electron in exactly the same way, then measure its position. You would get a hundred million numbers. Plot them as a histogram and the shape of that histogram is .
A single measurement gives you one definite position — not a blurred cloud. What is blurred is “where the next one will land”, not the electron itself.
The mathematics
The second equation is the normalizationThe requirement ∫|Ψ|²dx = 1, i.e. “the particle is definitely somewhere”. The Schrödinger equation guarantees that once normalised, always normalised.See 2.2 condition, discussed in the next section. It guarantees that “the particle is somewhere”.
Why it has to be the modulus squared
Squaring the modulus of a complex number looks like a technicality. In fact it solves two problems at once.
Why |Ψ|², and not Ψ or Re Ψbasic~4 min
A probability density has to satisfy two hard requirements:
- Non-negativity: . A probability cannot be negative.
- Room for interference: when contributions from two paths are added, cancellation must be possible.
Could we use directly? Solutions of the Schrödinger equation are generally complex, and can be negative or even imaginary, so requirement 1 is dead on arrival.
What about or ? Non-negativity can be forced by taking an absolute value, but that destroys requirement 2. The key point is that superposition happens at the level of , not at the level of . In the double slit,
so that
The last term is the interference term. In polar form it equals
and the phase difference decides whether it reinforces or cancels. If we added directly, would always exceed the sum of the parts and fringes could never appear.
So: complex numbers supply the phase, the phase supplies interference, and the modulus squared supplies a non-negative probability. All three are needed. This is also why quantum mechanics cannot do without complex numbers — they are not a mathematical convenience but a physical necessity.
Have a look
The simulation below shows a particle in a one-dimensional infinite square well. The purple curve is , and the area under it over any interval is the probability of finding the particle there. The well itself is not solved until section 2.7; here only one thing matters: the blue curve () can be positive or negative, the purple one () never is.
The infinite square well
Drag the width L and the quantum number n and watch the energy, the waveform and the probability distribution move together. Units: ħ = m = 1.
- Energy Eₙ (n=1)
- 4.935
- relative to E₁(L=1)
- 1.00 ×
- ⟨x⟩ / L
- 0.500
- Δx / L
- 0.180
Shrink the box and every level is pushed up together: E ∝ 1/L²
nodes = n − 1 = 0 (endpoints excluded)
Try this
- Drag
Lfrom 2.5 down to 0.6 and keep your eye on the dashed line in the level diagram (pinned at the reference energy E₁(L=1)): it sinks all the way to the bottom, meaning every level has risen far above it. The "relative to E₁(L=1)" readout climbs from 0.16 to 2.78 — "the tighter you confine a particle, the more kinetic energy it has", a direct consequence ofΔxΔp ≥ ħ/2. - Change
nin the stationary mode and note that|ψ|²never changes with time (the curve stands still); switch to a superposition, press play, and|ψ|²immediately starts sloshing. That is exactly what "stationary" refers to. - Leave only c₁ in the superposition (drag the rest to 0) and press play — the probability density stops moving again. However long a single eigenstate evolves, it only picks up an overall phase
e^(−iEₙt/ħ), which no observable can see. - Push n above 10 and look at
|ψ|²: the fringes get so fine that the distribution is nearly uniform — the classical picture of a particle equally likely to be anywhere in the box. The correspondence principle, in view.
Turn the quantum number up to 3 and you will see cross zero twice inside the well. At those zeros the probability of finding the particle is exactly zero — even though there is substantial probability on both sides. A classical particle bouncing around a box could never manage to “never pass through some intermediate position”. That is already a strong quantum effect.
A concrete calculation
Worked example: probability over an intervalbasic~5 min
Take a particle with wavefunction
Step 1: fix the normalisation constant .
Term by term:
Step 2: find the probability in the left quarter.
Over the common denominator 15360: , so
About 10.4%. For comparison, a uniform distribution would give 25% over the same interval — this wavefunction pushes the particle towards the middle, because it vanishes at both ends.
Key formulas
Born rule
The only bridge between the wavefunction and experiment
Probability density
Dimensions of 1/length; ρ dx is the probability
Interference term
Superposition acts on Ψ; interference comes from the phase difference
Self-check3 questions
- 1.
A wavefunction satisfies Ψ(x₀) = −0.4 (units suppressed). Which statement about the probability density near x₀ is correct?
- 2.
Why must a quantum wavefunction be allowed to take complex values? (Select all that apply.)
Select all that apply
- 3.
For Ψ(x) = A·x(L−x) on 0 ≤ x ≤ L (zero elsewhere) with L = 1, find the probability of the particle lying in [0, 0.25] (three decimal places).
3% relative tolerance
What comes next
The condition in the Born rule is not something imposed by hand — it has to hold at every instant, or particles would vanish into thin air. The next section proves that the Schrödinger equation guarantees exactly this, and picks up a quantity describing “where the probability is flowing” along the way.
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